Species

KNApSAcK Entry

Organism name Cladrastis sikokiana
Genus Cladrastis
Family Fabaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Cladrastis sikokiana
Linked NCBI taxonomy ID 53857
Linked level species

Family

Family in NCBI taxonomy Fabaceae
ID 3803

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Metabolite list (14)

KNApSAcK ID name ChEMBL link CTD link # of proteins in
ChEMBL interaction
/ related OMIM
/ related KEGG DISEASE
# of genes in
CTD interaction
/ related diseases
KCF-S
cluster
phytochemical
cluster
figure
C00010096 External link 512 8-O-Methylretusin 7-O-laminaribioside
No. 1 No. 15
C00010135 External link 512 Platycarpanetin 7-O-glucoside
No. 2 No. 15
C00010097 External link 512 Fujikinetin 7-O-glucoside
/ 7-Hydroxy-6'-methoxy-3',4'-methylenedioxyisoflavone 7-O-glucoside
No. 2 No. 15
C00010085 External link 512 Rothindin
/ Pseudobaptigenin 7-O-glucoside
No. 2 No. 15
C00010095 External link 512 8-O-Methylretusin 7-O-glucoside
No. 2 No. 15
C00002525 External link 512 Formononetin
/ 7-Hydroxy-4'-methoxyisoflavone
CHEMBL242341
C007768
24 / 36 / 58 13 / 0 No. 3 No. 15
C00009476 External link 512 Dipteryxine
/ Isoplatycarpanetin
/ 7-Hydroxy-5,6-dimethoxy-3',4'-methylenedioxyisoflavone
No. 27 No. 15
C00009478 External link 512 Platycarpanetin
No. 27 No. 15
C00002507 External link 512 Castanin
/ Afromosin
/ Afrormosin
/ 7-Hydroxy-6,4'-dimethoxyisoflavone
CHEMBL464404
C080240
7 / 14 / 39 1 / 0 No. 35 No. 15
C00009471 External link 512 Iso-5-methoxyafrormosin
/ 7-Hydroxy-5,8,4'-trimethoxyisoflavone
No. 35 No. 15
C00009470 External link 512 5-Methoxyafrormosin
/ 7-Hydroxy-5,6,4'-trimethoxyisoflavone
CHEMBL457449
No. 35 No. 15
C00009398 External link 512 Cladrin
/ 7-Hydroxy-3',4'-dimethoxyisoflavone
CHEMBL454746
13 / 31 / 49 No. 35 No. 15
C00009415 External link 512 Cladrastin
No. 35 No. 15
C00009538 External link 512 3'-Methoxydihydroformononetin
/ 7-Hydroxy-3',4'-dimethoxyisoflavanone
No. 106 No. 14

Human Protein / Gene in interactions

33 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P04637 Cellular tumor antigen p53 Transcription Factor C00002507 C00002525 C00009398 7 / 37
P38398 Breast cancer type 1 susceptibility protein Enzyme C00002507 C00002525 C00009398 4 / 2
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00002507 C00009398 0 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00002525 C00009398 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00002525 C00009398 4 / 3
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00002525 C00009398 3 / 3
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00002525 C00009398 5 / 3
B2RXH2 Lysine-specific demethylase 4E Enzyme C00002525 C00009398 0 / 0
P51151 Ras-related protein Rab-9A Unclassified protein C00002507 C00009398 0 / 0
P11021 78 kDa glucose-regulated protein Unclassified protein C00002525 0 / 0
P17405 Sphingomyelin phosphodiesterase Enzyme C00002507 2 / 2
O75496 Geminin Unclassified protein C00002507 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00002525 0 / 1
P04798 Cytochrome P450 1A1 Cytochrome P450 1A1 C00002525 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00009398 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00009398 7 / 3
P00352 Retinal dehydrogenase 1 Enzyme C00002525 0 / 0
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 C00002525 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00009398 0 / 0
Q16637 Survival motor neuron protein Unclassified protein C00002525 4 / 1
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00002525 2 / 2
O15118 Niemann-Pick C1 protein Unclassified protein C00009398 1 / 1
P31639 Sodium/glucose cotransporter 2 Glucose C00002525 1 / 1
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00002525 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002525 0 / 1
P13866 Sodium/glucose cotransporter 1 Glucose C00002525 1 / 1
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00002525 0 / 0
Q07869 Peroxisome proliferator-activated receptor alpha NR1C1 C00002525 0 / 0
P33527 Multidrug resistance-associated protein 1 drugs C00002525 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00002507 1 / 0
O00255 Menin Unclassified protein C00002525 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00002525 1 / 2
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00002525 1 / 0

13 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
4363 ABCC1, ABC29, ABCC, GS-X, MRP, MRP1 ATP-binding cassette, sub-family C (CFTR/MRP), member 1 C00002507 C00002525
2100 ESR2, ER-BETA, ESR-BETA, ESRB, ESTRB, Erb, NR3A2 estrogen receptor 2 (ER beta) C00002525
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00002525
1545 CYP1B1, CP1B, CYPIB1, GLC3A, P4501B1 cytochrome P450, family 1, subfamily B, polypeptide 1 (EC:1.14.14.1) C00002525
2056 EPO, EP, MVCD2 erythropoietin C00002525
2099 ESR1, ER, ESR, ESRA, ESTRR, Era, NR3A1 estrogen receptor 1 C00002525
5243 ABCB1, ABC20, CD243, CLCS, GP170, MDR1, P-GP, PGY1 ATP-binding cassette, sub-family B (MDR/TAP), member 1 (EC:3.6.3.44) C00002525
3091 HIF1A, HIF-1A, HIF-1alpha, HIF1, HIF1-ALPHA, MOP1, PASD8, bHLHe78 hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor) C00002525
54658 UGT1A1, BILIQTL1, GNT1, HUG-BR1, UDPGT, UDPGT_1-1, UGT1, UGT1A UDP glucuronosyltransferase 1 family, polypeptide A1 (EC:2.4.1.17) C00002525
54575 UGT1A10, UDPGT, UGT-1J, UGT1-10, UGT1.10, UGT1J UDP glucuronosyltransferase 1 family, polypeptide A10 (EC:2.4.1.17) C00002525
54577 UGT1A7, UDPGT, UDPGT_1-7, UGT-1G, UGT1-07, UGT1.7, UGT1G UDP glucuronosyltransferase 1 family, polypeptide A7 (EC:2.4.1.17) C00002525
54576 UGT1A8, UDPGT, UDPGT_1-8, UGT-1H, UGT1-08, UGT1.8, UGT1A8S, UGT1H UDP glucuronosyltransferase 1 family, polypeptide A8 (EC:2.4.1.17) C00002525
54600 UGT1A9, HLUGP4, LUGP4, UDPGT, UDPGT_1-9, UGT-1I, UGT1-09, UGT1-9, UGT1.9, UGT1AI, UGT1I UDP glucuronosyltransferase 1 family, polypeptide A9 (EC:2.4.1.17) C00002525

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (46)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
%606641 Body mass index; bmi P37231
#114480 Breast cancer P38398
#604370 Breast-ovarian cancer, familial, susceptibility to, 1; brovca1 P38398
#609338 Carotid intimal medial thickness 1 P37231
#119900 Digital clubbing, isolated congenital P15428
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#133239 Esophageal cancer P04637
#600274 Frontotemporal dementia; ftd P10636
#137800 Glioma susceptibility 1; glm1 O75874
P37231
#606824 Glucose/galactose malabsorption; ggm P13866
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#604367 Lipodystrophy, familial partial, type 3; fpld3 P37231
#211980 Lung cancer P04637
#174800 Mccune-albright syndrome; mas P63092
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#257220 Niemann-pick disease, type c1; npc1 O15118
#601665 Obesity P37231
#166350 Osseous heteroplasia, progressive; poh P63092
#167000 Ovarian cancer P38398
#614320 Pancreatic cancer, susceptibility to, 4; pnca4 P38398
#260500 Papilloma of choroid plexus; cpp P04637
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#102200 Pituitary adenoma, growth hormone-secreting P63092
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#233100 Renal glucosuria; glys1 P31639
#253300 Spinal muscular atrophy, type i; sma1 Q16637
#253550 Spinal muscular atrophy, type ii; sma2 Q16637
#253400 Spinal muscular atrophy, type iii; sma3 Q16637
#271150 Spinal muscular atrophy, type iv; sma4 Q16637
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (64)

KEGG name UniProt
H00033 Adrenal carcinoma O00255 (related)
P04637 (related)
H00034 Carcinoid O00255 (related)
H00045 Malignant islet cell carcinoma O00255 (related)
H00246 Primary hyperparathyroidism O00255 (related)
H01102 Pituitary adenomas O00255 (related)
H00136 Niemann-Pick disease type C (NPC) O15118 (related)
H00004 Chronic myeloid leukemia (CML) P04637 (related)
H00005 Chronic lymphocytic leukemia (CLL) P04637 (related)
H00006 Hairy-cell leukemia P04637 (related)
H00008 Burkitt lymphoma P04637 (related)
H00009 Adult T-cell leukemia P04637 (related)
H00010 Multiple myeloma P04637 (related)
H00013 Small cell lung cancer P04637 (related)
H00014 Non-small cell lung cancer P04637 (related)
H00015 Malignant pleural mesothelioma P04637 (related)
H00016 Oral cancer P04637 (related)
P04637 (marker)
H00017 Esophageal cancer P04637 (related)
P04637 (marker)
H00018 Gastric cancer P04637 (related)
H00019 Pancreatic cancer P04637 (related)
P04637 (marker)
H00020 Colorectal cancer P04637 (related)
P04637 (marker)
H00022 Bladder cancer P04637 (related)
H00025 Penile cancer P04637 (related)
P04637 (marker)
H00026 Endometrial Cancer P04637 (related)
H00027 Ovarian cancer P04637 (related)
P38398 (related)
H00028 Choriocarcinoma P04637 (related)
H00029 Vulvar cancer P04637 (related)
H00031 Breast cancer P04637 (related)
P38398 (related)
H00032 Thyroid cancer P04637 (related)
P37231 (related)
H00036 Osteosarcoma P04637 (related)
P08684 (marker)
H00038 Malignant melanoma P04637 (related)
H00039 Basal cell carcinoma P04637 (related)
H00040 Squamous cell carcinoma P04637 (related)
H00041 Kaposi's sarcoma P04637 (related)
H00042 Glioma P04637 (related)
P04637 (marker)
H00044 Cancer of the anal canal P04637 (related)
H00046 Cholangiocarcinoma P04637 (related)
H00047 Gallbladder cancer P04637 (related)
H00048 Hepatocellular carcinoma P04637 (related)
H00055 Laryngeal cancer P04637 (related)
P04637 (marker)
H00881 Li-Fraumeni syndrome P04637 (related)
H01007 Choroid plexus papilloma P04637 (related)
H00021 Renal cell carcinoma P04637 (marker)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H01205 Coumarin resistance P11712 (related)
H01261 Congenital glucose-galactose malabsorption (GGM) P13866 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00137 Niemann-Pick disease (NPD) typeA and B P17405 (related)
H00424 Defects in the degradation of sphingomyelin P17405 (related)
H01126 Familial renal glucosuria (FRG) P31639 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00409 Type II diabetes mellitus P37231 (related)
H00420 Familial partial lipodystrophy (FPL) P37231 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q03164 (related)
Q03164 (marker)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)
H00480 Non-syndromic X-linked mental retardation Q99714 (related)
H00658 Syndromic X-linked mental retardation Q99714 (related)
H00925 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency Q99714 (related)